Synthetic styrene-based bioinspired model of the [FeFe]-hydrogenase active site for electrocatalytic hydrogen evolution.

Autor: Zamader A; Univ Grenoble Alpes, CNRS, CEA, IRIG, Laboratoire de Chimie et Biologie des Métaux 17 rue des Martyrs 38000 Grenoble France bertrand.reuillard@cea.fr.; Department of Chemistry - Ångström Laboratory, Uppsala University Box 523 SE-75120 Uppsala Sweden gustav.berggren@kemi.uu.se., Reuillard B; Univ Grenoble Alpes, CNRS, CEA, IRIG, Laboratoire de Chimie et Biologie des Métaux 17 rue des Martyrs 38000 Grenoble France bertrand.reuillard@cea.fr., Pérard J; Univ Grenoble Alpes, CNRS, CEA, IRIG, Laboratoire de Chimie et Biologie des Métaux 17 rue des Martyrs 38000 Grenoble France bertrand.reuillard@cea.fr., Billon L; Universite de Pau et Pays de l'Adour, E2S UPPA, IPREM, Bio-inspired Materials Group: Functionalities & Self-Assembly 2 avenue Angot 64053 Pau France., Berggren G; Department of Chemistry - Ångström Laboratory, Uppsala University Box 523 SE-75120 Uppsala Sweden gustav.berggren@kemi.uu.se., Artero V; Univ Grenoble Alpes, CNRS, CEA, IRIG, Laboratoire de Chimie et Biologie des Métaux 17 rue des Martyrs 38000 Grenoble France bertrand.reuillard@cea.fr.
Jazyk: angličtina
Zdroj: Sustainable energy & fuels [Sustain Energy Fuels] 2023 Aug 23; Vol. 7 (19), pp. 4967-4976. Date of Electronic Publication: 2023 Aug 23 (Print Publication: 2023).
DOI: 10.1039/d3se00409k
Abstrakt: Integration of molecular catalysts inside polymeric scaffolds has gained substantial attention over the past decade, as it provides a path towards generating systems with enhanced stability as well as enzyme-like morphologies and properties. In the context of solar fuels research and chemical energy conversion, this approach has been found to improve both rates and energy efficiencies of a range of catalytic reactions. However, system performance still needs to be improved to reach technologically relevant currents and stability, parameters that are heavily influenced by the nature of the incorporated molecular catalyst. Here, we have focused on the integration of a biomimetic {Fe 2 (μ-adt)(CO) 6 } (-CH 2 NHCH 2 S-, azadithiolate or adt 2- ) based active site ("[2Fe2S] adt "), inspired by the catalytic cofactor of [FeFe] hydrogenases, within a synthetic polymeric scaffold using free radical polymerization. The resulting metallopolymers [2Fe2S] adt k [DMAEMA] l [PyBMA] m (DMAEMA = dimethylaminoethyl methacrylate as water soluble monomer; PyBMA = 4-(pyren-1-yl)-butyl methacrylate as hydrophobic anchor for heterogenization) were found to be active for electrochemical H 2 production in neutral aqueous media. The pyrene content was varied to optimize durability and activity. Following immobilization on multiwalled carbon nanotubes (MWNT) the most active metallopolymer, containing ∼2.3 mol% of PyBMA, could reach a turnover number for hydrogen production (TON H 2 ) of ∼0.4 ×10 5 over 20 hours of electrolysis at an overpotential of 0.49 V, two orders of magnitude higher than the isolated catalyst counterpart. The study provides a synthetic methodology for incorporating catalytic units featuring second coordination sphere functional groups, and highlights the benefit of the confinement within the polymer matrix for catalytic performance.
Competing Interests: There are no conflicts to declare.
(This journal is © The Royal Society of Chemistry.)
Databáze: MEDLINE
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